Also known as: Galactosemia screen, GALT or Gal-1-PUT
- Clouding of the lens of the eye (cataracts)
- Scarring of the liver (cirrhosis)
- Failure to thrive
- Yellow color of the skin or eyes (jaundice)
- Liver enlargement
- Intellectual disability
- Excessive bleeding
- Fainting or feeling lightheaded
- Hematoma (blood accumulating under the skin, causing bruising)
- Infection (a slight risk any time the skin is broken)
Galactose-1-phosphate uridyltransferase is a blood test that measures the level of a substance called GALT, which helps break down milk sugars in your body. A low level of this substance causes a condition called galactosemia.
How the Test is Performed
A blood sample is needed.
How the Test will Feel
When the needle is inserted to draw blood, some infants feel moderate pain. Others feel only a prick or stinging. Afterward, there may be slight bruising. This soon goes away.
Why the Test is Performed
This is a screening test for galactosemia.
In normal diets, most galactose comes from the breakdown (metabolism) of lactose, which is found in milk and dairy products. 1 out of 65,000 newborns lack a substance (enzyme) called GALT. Without this substance, the body cannot break down galactose, and the substance builds up in the blood. Continued use of milk products can lead to:
This can be a serious condition if not treated.
Every state requires newborn screening tests to check for this disorder.
The normal range is 18.5 to 28.5 U/g Hb (units per gram of hemoglobin).
Normal value ranges may vary slightly among different laboratories. Some labs use different measurements or may test different samples. Talk to your doctor about the meaning of your specific test results.
What Abnormal Results Mean
An abnormal result suggests galactosemia. Further tests must be done to confirm the diagnosis.
If your child has galactosemia, a genetics specialist should be consulted promptly. The child should immediately be placed on a no-milk diet. This means no breast milk and no animal milk. Soy milk and infant soy formulas are generally used as substitutes.
This test is very sensitive, so it does not miss many infants with galactosemia. But, false-positives can occur. If your child has an abnormal screening result, follow-up tests must be done to confirm the result.
Veins and arteries vary in size from one infant to another and from one side of the body to the other. Obtaining a blood sample from some infants may be more difficult than from others.
Other risks associated with having blood drawn are slight but may include:
Kishnani PS. Defects in metabolism of carbohydrates. In: Kliegman RM, Stanton BF, St. Geme J III, Schor N, Behrman RE, eds. Nelson Textbook of Pediatrics. 19th ed. Philadelphia, PA: Elsevier Saunders; 2011:chap 81.
- Review date:
- December 07, 2016
- Reviewed by:
- Chad Haldeman-Englert, MD, FACMG, Wake Forest School of Medicine, Department of Pediatrics, Section on Medical Genetics, Winston-Salem, NC. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editorial team.
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